Taxuspin F

Details

Top
Internal ID 3c79bbd1-0886-4595-8c7a-6fadc39b696d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Taxanes and derivatives
IUPAC Name [(1R,2R,3R,5S,7S,8S,9R,10R)-2,9,10-triacetyloxy-5-hydroxy-8,12,15,15-tetramethyl-4-methylidene-13-oxo-7-tricyclo[9.3.1.03,8]pentadec-11-enyl] acetate
SMILES (Canonical) CC1=C2C(C(C3(C(CC(C(=C)C3C(C(C2(C)C)CC1=O)OC(=O)C)O)OC(=O)C)C)OC(=O)C)OC(=O)C
SMILES (Isomeric) CC1=C2[C@H]([C@@H]([C@@]3([C@H](C[C@@H](C(=C)[C@H]3[C@@H]([C@@H](C2(C)C)CC1=O)OC(=O)C)O)OC(=O)C)C)OC(=O)C)OC(=O)C
InChI InChI=1S/C28H38O10/c1-12-19(33)10-18-24(36-15(4)30)23-13(2)20(34)11-21(35-14(3)29)28(23,9)26(38-17(6)32)25(37-16(5)31)22(12)27(18,7)8/h18,20-21,23-26,34H,2,10-11H2,1,3-9H3/t18-,20-,21-,23-,24+,25+,26-,28+/m0/s1
InChI Key CWMUWKWZNUFEDY-LCFONYPQSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C28H38O10
Molecular Weight 534.60 g/mol
Exact Mass 534.24649740 g/mol
Topological Polar Surface Area (TPSA) 143.00 Ų
XlogP 1.40
Atomic LogP (AlogP) 2.60
H-Bond Acceptor 10
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

Top
CHEMBL310157
164991-80-4

2D Structure

Top
2D Structure of Taxuspin F

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9940 99.40%
Caco-2 - 0.6857 68.57%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.7493 74.93%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8416 84.16%
OATP1B3 inhibitior + 0.8850 88.50%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.5333 53.33%
P-glycoprotein inhibitior + 0.7799 77.99%
P-glycoprotein substrate - 0.6464 64.64%
CYP3A4 substrate + 0.6782 67.82%
CYP2C9 substrate - 0.7791 77.91%
CYP2D6 substrate - 0.8979 89.79%
CYP3A4 inhibition - 0.5977 59.77%
CYP2C9 inhibition - 0.8885 88.85%
CYP2C19 inhibition - 0.8674 86.74%
CYP2D6 inhibition - 0.9066 90.66%
CYP1A2 inhibition - 0.8584 85.84%
CYP2C8 inhibition + 0.4508 45.08%
CYP inhibitory promiscuity - 0.9403 94.03%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9043 90.43%
Carcinogenicity (trinary) Non-required 0.5779 57.79%
Eye corrosion - 0.9857 98.57%
Eye irritation - 0.8564 85.64%
Skin irritation - 0.5193 51.93%
Skin corrosion - 0.9386 93.86%
Ames mutagenesis - 0.8215 82.15%
Human Ether-a-go-go-Related Gene inhibition - 0.6045 60.45%
Micronuclear - 0.6000 60.00%
Hepatotoxicity + 0.6231 62.31%
skin sensitisation + 0.5283 52.83%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity + 0.6556 65.56%
Acute Oral Toxicity (c) III 0.5785 57.85%
Estrogen receptor binding + 0.7436 74.36%
Androgen receptor binding + 0.6658 66.58%
Thyroid receptor binding + 0.5143 51.43%
Glucocorticoid receptor binding + 0.6885 68.85%
Aromatase binding + 0.5490 54.90%
PPAR gamma + 0.7366 73.66%
Honey bee toxicity - 0.6082 60.82%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9885 98.85%

Targets

Top

Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.92% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.38% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.28% 85.14%
CHEMBL340 P08684 Cytochrome P450 3A4 88.89% 91.19%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 87.92% 82.69%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.75% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.96% 86.33%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 86.84% 81.11%
CHEMBL2581 P07339 Cathepsin D 86.61% 98.95%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.68% 95.50%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.47% 100.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.14% 99.23%
CHEMBL2996 Q05655 Protein kinase C delta 84.63% 97.79%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.21% 94.45%
CHEMBL1937 Q92769 Histone deacetylase 2 83.79% 94.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.27% 94.00%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 82.17% 93.03%
CHEMBL5028 O14672 ADAM10 80.58% 97.50%

Plants that contains it

Top
Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Taxus canadensis
Taxus cuspidata
Taxus wallichiana

Cross-Links

Top
PubChem 10347049
NPASS NPC143609
LOTUS LTS0021135
wikiData Q104971392